Nitroglycerin Structural Formula (Image 01)
Nitroglycerin In Dextrose Injection
Product Images NDC 0338-1051
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Nitroglycerin In Dextrose (NDC 0338-1051). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Baxter Healthcare Company, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Dextrose Structural Formula (Image 02)
Representative Container 25 mg Nitroglycerin, 0338-1047-02 (Image 03)
Nitroglycerin in 6% Dextrose Injection is a medication with a concentration of 25mg per 250mL and contains 6% dextrose. The medication is manufactured by Baxter and is identified by the NDC code 0338-1047-02. The remaining text is not-readable.*
Representative Carton Label (25 mg Nitroglycerin 0338-1047-02)
This is a label for an injection containing 25 mg of Nitroglycerin in 5% Dextrose solution with an expiration date and LOT number. The NDC number is 0338-1047-02 and the product code is 1A0692.*
Representative Nitroglycerin In Dextrose Serialization Label 0338-1047-02 (Image 05)
This is a description of an injection of 25 mg Nitroglycerin in 5% Dextrose that comes in a 250 ml bottle. It includes information such as the product code (NDC 0338-1047-02), the lot number (G222009), and expiration date (OGT 17). The text also includes a unique identifier (01) 50303381047028 and a additional codes (21) 36174 and (17) 171031.*
Representative Container_50 mg Nitroglycerin, Ndc 0338-1049-02 (Image 06)
This is a label for Nitroglycerin in 5% Dextrose Injection with a concentration of 50 mg per 250 mL and an NDC number of 0338-1049-02. The label includes some inconclusive characters and some misread characters.*
Representative Carton Label, 50 mg Nitroglycerin (Image 07)
This is a medication label for Nitroglycerin, an injection administered via 5% Dextrose solution. The label includes the medication strength of 50mg and the National Drug Code identifier of 0338 — 104902 1A0694. It also includes an expiration date (EXP) and lot number details.*
Representative Nitroglycerin In Dextrose Serialization Label 0338-1049-02 (Image 08)
This is a description of a medication called Nitroglycerin. It is available as an injection with a concentration of 50 mg in 5% dextrose solution, which comes in a 250 ml container. The NDC number is 0338-1049-02, with the lot number G888852 and an expiration date of January of 2018.*
Representative Container Label_100 mg Nitroglycerin, 0338-1051-02 (Image 09)
This text appears to be a medication label for a solution containing Nitroglycerin and Dextrose. It has information about the dosage strength, NDC code, and an address for Baxter.*
Representative Carton Label, 100 mg Nitroglycerin (Image 10)
This is a medication package containing an injection of Nitroglycerin in 5% Dextrose with a quantity of 100mg. It has an NDC (National Drug Code) number of 0338-1051-02 and an EXP LOT #. The rest of the text is possibly to identify the medication or its components but it is not legible.*
Representative Nitroglycerin In Dextrose Serialization Label 0338-1051-02 (Image 11)
This is a description of a medication, specifically an injection that contains 100 mg of Nitroglycerin and is mixed with 5% Dextrose in a 250 ml 12 Injection. The National Drug Code for this medication is 0338105102 (01) 50303381051028. There are also lot and expiration date details provided. However, there is missing information needed to create a complete description, and the content may need verification for typographical errors.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
